CA2406968C - Method of controlling zoological and aquatic plant growth - Google Patents

Method of controlling zoological and aquatic plant growth Download PDF

Info

Publication number: CA2406968C
Authority: CA; Canada
Prior art keywords: water; methyl; compound; ppm; naphthalenedione
Prior art date: 2000-02-17
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Expired - Fee Related

Application number

CA2406968A

Other languages

English (en)

French (fr)

Other versions

CA2406968A1 (en

Inventor

Horace Cutler

Stephen Cutler

David Wright

Rodger Dawson

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Garnett Inc

Original Assignee

Garnett Inc

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

2000-02-17

Filing date

2001-02-16

Publication date

2011-07-05

2000-02-17 Priority claimed from US09/506,017 external-priority patent/US6340468B1/en

2001-02-16 Application filed by Garnett Inc filed Critical Garnett Inc

2001-08-23 Publication of CA2406968A1 publication Critical patent/CA2406968A1/en

2011-07-05 Application granted granted Critical

2011-07-05 Publication of CA2406968C publication Critical patent/CA2406968C/en

2021-02-16 Anticipated expiration legal-status Critical

Status Expired - Fee Related legal-status Critical Current

Links

238000000034 method Methods 0.000 title claims abstract description 47
230000008635 plant growth Effects 0.000 title description 2
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 102
150000001875 compounds Chemical class 0.000 claims abstract description 54
231100000331 toxic Toxicity 0.000 claims abstract description 46
230000002588 toxic effect Effects 0.000 claims abstract description 46
241000607479 Yersinia pestis Species 0.000 claims abstract description 40
241001465754 Metazoa Species 0.000 claims abstract description 29
244000005700 microbiome Species 0.000 claims abstract description 23
239000001257 hydrogen Substances 0.000 claims description 23
229910052739 hydrogen Inorganic materials 0.000 claims description 23
-1 chloro, acetonyl Chemical group 0.000 claims description 13
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 13
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 13
241000237852 Mollusca Species 0.000 claims description 11
FRASJONUBLZVQX-UHFFFAOYSA-N 1,4-naphthoquinone Chemical compound C1=CC=C2C(=O)C=CC(=O)C2=C1 FRASJONUBLZVQX-UHFFFAOYSA-N 0.000 claims description 9
MJVAVZPDRWSRRC-UHFFFAOYSA-N Menadione Chemical compound C1=CC=C2C(=O)C(C)=CC(=O)C2=C1 MJVAVZPDRWSRRC-UHFFFAOYSA-N 0.000 claims description 9
VCMMXZQDRFWYSE-UHFFFAOYSA-N Plumbagin Natural products C1=CC=C2C(=O)C(C)=CC(=O)C2=C1O VCMMXZQDRFWYSE-UHFFFAOYSA-N 0.000 claims description 7
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 6
CIEYTVIYYGTCCI-UHFFFAOYSA-N lapachol Chemical compound C1=CC=C2C(=O)C(CC=C(C)C)=C(O)C(=O)C2=C1 CIEYTVIYYGTCCI-UHFFFAOYSA-N 0.000 claims description 4
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 4
125000001844 prenyl group Chemical group [H]C([*])([H])C([H])=C(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 4
229940041603 vitamin k 3 Drugs 0.000 claims description 4
SVPKNMBRVBMTLB-UHFFFAOYSA-N 2,3-dichloronaphthalene-1,4-dione Chemical compound C1=CC=C2C(=O)C(Cl)=C(Cl)C(=O)C2=C1 SVPKNMBRVBMTLB-UHFFFAOYSA-N 0.000 claims description 2
MNQDVQOXHPDHPT-UHFFFAOYSA-N 5,8-dihydroxy-7-methoxy-2-(2-oxopropyl)naphthalene-1,4-dione Chemical compound O=C1C=C(CC(C)=O)C(=O)C2=C(O)C(OC)=CC(O)=C21 MNQDVQOXHPDHPT-UHFFFAOYSA-N 0.000 claims description 2
230000002147 killing effect Effects 0.000 claims description 2
LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical group OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 claims 3
YZACZIYTZCJVSN-UHFFFAOYSA-N Chimaphylin Chemical compound C1=C(C)C=C2C(=O)C(C)=CC(=O)C2=C1 YZACZIYTZCJVSN-UHFFFAOYSA-N 0.000 claims 1
241000425347 Phyla <beetle> Species 0.000 claims 1
241000894006 Bacteria Species 0.000 abstract description 16
AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 abstract description 14
KETQAJRQOHHATG-UHFFFAOYSA-N 1,2-naphthoquinone Chemical class C1=CC=C2C(=O)C(=O)C=CC2=C1 KETQAJRQOHHATG-UHFFFAOYSA-N 0.000 abstract description 9
150000004056 anthraquinones Chemical class 0.000 abstract description 8
150000004053 quinones Chemical class 0.000 abstract description 8
KEQHJBNSCLWCAE-UHFFFAOYSA-N thymoquinone Chemical compound CC(C)C1=CC(=O)C(C)=CC1=O KEQHJBNSCLWCAE-UHFFFAOYSA-N 0.000 abstract description 7
LOUPRKONTZGTKE-WZBLMQSHSA-N Quinine Chemical compound C([C@H]([C@H](C1)C=C)C2)C[N@@]1[C@@H]2[C@H](O)C1=CC=NC2=CC=C(OC)C=C21 LOUPRKONTZGTKE-WZBLMQSHSA-N 0.000 abstract description 5
ZYGHJZDHTFUPRJ-UHFFFAOYSA-N benzo-alpha-pyrone Natural products C1=CC=C2OC(=O)C=CC2=C1 ZYGHJZDHTFUPRJ-UHFFFAOYSA-N 0.000 abstract description 5
LOUPRKONTZGTKE-UHFFFAOYSA-N cinchonine Natural products C1C(C(C2)C=C)CCN2C1C(O)C1=CC=NC2=CC=C(OC)C=C21 LOUPRKONTZGTKE-UHFFFAOYSA-N 0.000 abstract description 3
PJVWKTKQMONHTI-UHFFFAOYSA-N warfarin Chemical compound OC=1C2=CC=CC=C2OC(=O)C=1C(CC(=O)C)C1=CC=CC=C1 PJVWKTKQMONHTI-UHFFFAOYSA-N 0.000 abstract description 3
235000001258 Cinchona calisaya Nutrition 0.000 abstract description 2
GIIGAFADHXYOPM-UHFFFAOYSA-N amphotalide Chemical compound C1=CC(N)=CC=C1OCCCCCN1C(=O)C2=CC=CC=C2C1=O GIIGAFADHXYOPM-UHFFFAOYSA-N 0.000 abstract description 2
229950008495 amphotalide Drugs 0.000 abstract description 2
235000001671 coumarin Nutrition 0.000 abstract description 2
229960000948 quinine Drugs 0.000 abstract description 2
229960005080 warfarin Drugs 0.000 abstract description 2
150000004775 coumarins Chemical class 0.000 abstract 1
SXWPCWBFJXDMAI-UHFFFAOYSA-L disodium;3,4,5,6-tetraoxocyclohexene-1,2-diolate Chemical compound [Na+].[Na+].[O-]C1=C([O-])C(=O)C(=O)C(=O)C1=O SXWPCWBFJXDMAI-UHFFFAOYSA-L 0.000 abstract 1
241000196324 Embryophyta Species 0.000 description 31
241000894007 species Species 0.000 description 25
241000193901 Dreissena polymorpha Species 0.000 description 23
241000237858 Gastropoda Species 0.000 description 18
238000003556 assay Methods 0.000 description 18
241000199914 Dinophyceae Species 0.000 description 17
238000011282 treatment Methods 0.000 description 17
238000012360 testing method Methods 0.000 description 16
239000000203 mixture Substances 0.000 description 14
241001501885 Isochrysis Species 0.000 description 13
230000012010 growth Effects 0.000 description 11
210000004027 cell Anatomy 0.000 description 10
241000015682 Eurytemora affinis Species 0.000 description 9
235000013601 eggs Nutrition 0.000 description 9
NJWGQARXZDRHCD-UHFFFAOYSA-N 2-methylanthraquinone Chemical compound C1=CC=C2C(=O)C3=CC(C)=CC=C3C(=O)C2=C1 NJWGQARXZDRHCD-UHFFFAOYSA-N 0.000 description 8
VTWDKFNVVLAELH-UHFFFAOYSA-N 2-methylcyclohexa-2,5-diene-1,4-dione Chemical compound CC1=CC(=O)C=CC1=O VTWDKFNVVLAELH-UHFFFAOYSA-N 0.000 description 8
241000195493 Cryptophyta Species 0.000 description 8
241000237502 Ostreidae Species 0.000 description 8
150000002431 hydrogen Chemical group 0.000 description 8
235000020636 oyster Nutrition 0.000 description 8
RGCKGOZRHPZPFP-UHFFFAOYSA-N alizarin Chemical compound C1=CC=C2C(=O)C3=C(O)C(O)=CC=C3C(=O)C2=C1 RGCKGOZRHPZPFP-UHFFFAOYSA-N 0.000 description 7
230000000694 effects Effects 0.000 description 7
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
241000238582 Artemia Species 0.000 description 6
241000237536 Mytilus edulis Species 0.000 description 6
LQGUBLBATBMXHT-UHFFFAOYSA-N chrysophanol Chemical compound C1=CC=C2C(=O)C3=CC(C)=CC(O)=C3C(=O)C2=C1O LQGUBLBATBMXHT-UHFFFAOYSA-N 0.000 description 6
235000013305 food Nutrition 0.000 description 6
210000001161 mammalian embryo Anatomy 0.000 description 6
239000003973 paint Substances 0.000 description 6
241000251468 Actinopterygii Species 0.000 description 5
241000239250 Copepoda Species 0.000 description 5
241000238424 Crustacea Species 0.000 description 5
241001466077 Salina Species 0.000 description 5
238000000576 coating method Methods 0.000 description 5
230000002401 inhibitory effect Effects 0.000 description 5
239000000463 material Substances 0.000 description 5
235000020638 mussel Nutrition 0.000 description 5
239000011734 sodium Substances 0.000 description 5
229910052708 sodium Inorganic materials 0.000 description 5
239000000126 substance Substances 0.000 description 5
241000195644 Neochloris Species 0.000 description 4
241000243142 Porifera Species 0.000 description 4
UIXPTCZPFCVOQF-UHFFFAOYSA-N Ubiquinone-O Natural products COC1=C(OC)C(=O)C(C)=CC1=O UIXPTCZPFCVOQF-UHFFFAOYSA-N 0.000 description 4
PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 4
238000004166 bioassay Methods 0.000 description 4
ATNHDLDRLWWWCB-AENOIHSZSA-M chlorophyll a Chemical compound C1([C@@H](C(=O)OC)C(=O)C2=C3C)=C2N2C3=CC(C(CC)=C3C)=[N+]4C3=CC3=C(C=C)C(C)=C5N3[Mg-2]42[N+]2=C1[C@@H](CCC(=O)OC\C=C(/C)CCC[C@H](C)CCC[C@H](C)CCCC(C)C)[C@H](C)C2=C5 ATNHDLDRLWWWCB-AENOIHSZSA-M 0.000 description 4
230000004720 fertilization Effects 0.000 description 4
KQPYUDDGWXQXHS-UHFFFAOYSA-N juglone Chemical compound O=C1C=CC(=O)C2=C1C=CC=C2O KQPYUDDGWXQXHS-UHFFFAOYSA-N 0.000 description 4
230000001418 larval effect Effects 0.000 description 4
230000007246 mechanism Effects 0.000 description 4
230000002265 prevention Effects 0.000 description 4
231100000419 toxicity Toxicity 0.000 description 4
230000001988 toxicity Effects 0.000 description 4
229940005561 1,4-benzoquinone Drugs 0.000 description 3
241000237519 Bivalvia Species 0.000 description 3
ACTIUHUUMQJHFO-UHFFFAOYSA-N Coenzym Q10 Natural products COC1=C(OC)C(=O)C(CC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)C)=C(C)C1=O ACTIUHUUMQJHFO-UHFFFAOYSA-N 0.000 description 3
241000192700 Cyanobacteria Species 0.000 description 3
239000005630 Diquat Substances 0.000 description 3
241000283070 Equus zebra Species 0.000 description 3
241000582055 Gymnocephalus cernua Species 0.000 description 3
206010061217 Infestation Diseases 0.000 description 3
241001501873 Isochrysis galbana Species 0.000 description 3
240000008415 Lactuca sativa Species 0.000 description 3
235000003228 Lactuca sativa Nutrition 0.000 description 3
241000295697 Pimephales promelas Species 0.000 description 3
241000242594 Platyhelminthes Species 0.000 description 3
241000243820 Polychaeta Species 0.000 description 3
239000003795 chemical substances by application Substances 0.000 description 3
229930002875 chlorophyll Natural products 0.000 description 3
235000019804 chlorophyll Nutrition 0.000 description 3
235000020639 clam Nutrition 0.000 description 3
239000011248 coating agent Substances 0.000 description 3
ACTIUHUUMQJHFO-UPTCCGCDSA-N coenzyme Q10 Chemical compound COC1=C(OC)C(=O)C(C\C=C(/C)CC\C=C(/C)CC\C=C(/C)CC\C=C(/C)CC\C=C(/C)CC\C=C(/C)CC\C=C(/C)CC\C=C(/C)CC\C=C(/C)CCC=C(C)C)=C(C)C1=O ACTIUHUUMQJHFO-UPTCCGCDSA-N 0.000 description 3
235000017471 coenzyme Q10 Nutrition 0.000 description 3
208000031513 cyst Diseases 0.000 description 3
210000002257 embryonic structure Anatomy 0.000 description 3
239000011521 glass Substances 0.000 description 3
230000009545 invasion Effects 0.000 description 3
KKZJGLLVHKMTCM-UHFFFAOYSA-N mitoxantrone Chemical compound O=C1C2=C(O)C=CC(O)=C2C(=O)C2=C1C(NCCNCCO)=CC=C2NCCNCCO KKZJGLLVHKMTCM-UHFFFAOYSA-N 0.000 description 3
229960001156 mitoxantrone Drugs 0.000 description 3
231100000706 no observed effect level Toxicity 0.000 description 3
NPCOQXAVBJJZBQ-UHFFFAOYSA-N reduced coenzyme Q9 Natural products COC1=C(O)C(C)=C(CC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)C)C(O)=C1OC NPCOQXAVBJJZBQ-UHFFFAOYSA-N 0.000 description 3
230000003068 static effect Effects 0.000 description 3
230000001954 sterilising effect Effects 0.000 description 3
231100000048 toxicity data Toxicity 0.000 description 3
229940035936 ubiquinone Drugs 0.000 description 3
239000002349 well water Substances 0.000 description 3
235000020681 well water Nutrition 0.000 description 3
BOCJQSFSGAZAPQ-UHFFFAOYSA-N 1-chloroanthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2Cl BOCJQSFSGAZAPQ-UHFFFAOYSA-N 0.000 description 2
OLBNOBQOQZRLMP-UHFFFAOYSA-N 2,6-dimethoxy-p-benzoquinone Chemical compound COC1=CC(=O)C=C(OC)C1=O OLBNOBQOQZRLMP-UHFFFAOYSA-N 0.000 description 2
HSHNITRMYYLLCV-UHFFFAOYSA-N 4-methylumbelliferone Chemical compound C1=C(O)C=CC2=C1OC(=O)C=C2C HSHNITRMYYLLCV-UHFFFAOYSA-N 0.000 description 2
ASDLSKCKYGVMAI-UHFFFAOYSA-N 9,10-dioxoanthracene-2-carboxylic acid Chemical compound C1=CC=C2C(=O)C3=CC(C(=O)O)=CC=C3C(=O)C2=C1 ASDLSKCKYGVMAI-UHFFFAOYSA-N 0.000 description 2
241000200031 Alexandrium Species 0.000 description 2
241000607620 Aliivibrio fischeri Species 0.000 description 2
241000243818 Annelida Species 0.000 description 2
241001302556 Bythotrephes longimanus Species 0.000 description 2
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
241000924360 Glenodinium Species 0.000 description 2
241000200139 Gonyaulax Species 0.000 description 2
241000200287 Gymnodinium Species 0.000 description 2
241000238631 Hexapoda Species 0.000 description 2
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
241000192701 Microcystis Species 0.000 description 2
241000200248 Prorocentrum Species 0.000 description 2
241001531268 Prorocentrum minimum Species 0.000 description 2
241000700141 Rotifera Species 0.000 description 2
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
241000607626 Vibrio cholerae Species 0.000 description 2
230000001154 acute effect Effects 0.000 description 2
238000013019 agitation Methods 0.000 description 2
RJGDLRCDCYRQOQ-UHFFFAOYSA-N anthrone Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3CC2=C1 RJGDLRCDCYRQOQ-UHFFFAOYSA-N 0.000 description 2
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
VYTBDSUNRJYVHL-UHFFFAOYSA-N beta-Hydrojuglone Natural products O=C1CCC(=O)C2=C1C=CC=C2O VYTBDSUNRJYVHL-UHFFFAOYSA-N 0.000 description 2
239000006227 byproduct Substances 0.000 description 2
VHRGRCVQAFMJIZ-UHFFFAOYSA-N cadaverine Chemical compound NCCCCCN VHRGRCVQAFMJIZ-UHFFFAOYSA-N 0.000 description 2
210000000038 chest Anatomy 0.000 description 2
239000003653 coastal water Substances 0.000 description 2
239000008199 coating composition Substances 0.000 description 2
238000001816 cooling Methods 0.000 description 2
230000005284 excitation Effects 0.000 description 2
230000003031 feeding effect Effects 0.000 description 2
239000013505 freshwater Substances 0.000 description 2
GSNBWTFAGXSQCO-UHFFFAOYSA-N fumigatin Chemical compound COC1=C(O)C(=O)C(C)=CC1=O GSNBWTFAGXSQCO-UHFFFAOYSA-N 0.000 description 2
238000004128 high performance liquid chromatography Methods 0.000 description 2
KQSBZNJFKWOQQK-UHFFFAOYSA-N hystazarin Natural products O=C1C2=CC=CC=C2C(=O)C2=C1C=C(O)C(O)=C2 KQSBZNJFKWOQQK-UHFFFAOYSA-N 0.000 description 2
238000001727 in vivo Methods 0.000 description 2
230000033001 locomotion Effects 0.000 description 2
229910052751 metal Inorganic materials 0.000 description 2
239000002184 metal Substances 0.000 description 2
230000005012 migration Effects 0.000 description 2
238000013508 migration Methods 0.000 description 2
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 2
231100000252 nontoxic Toxicity 0.000 description 2
230000003000 nontoxic effect Effects 0.000 description 2
239000001301 oxygen Substances 0.000 description 2
229910052760 oxygen Inorganic materials 0.000 description 2
244000045947 parasite Species 0.000 description 2
244000052769 pathogen Species 0.000 description 2
NFBAXHOPROOJAW-UHFFFAOYSA-N phenindione Chemical compound O=C1C2=CC=CC=C2C(=O)C1C1=CC=CC=C1 NFBAXHOPROOJAW-UHFFFAOYSA-N 0.000 description 2
230000008569 process Effects 0.000 description 2
238000012545 processing Methods 0.000 description 2
150000003839 salts Chemical class 0.000 description 2
239000013049 sediment Substances 0.000 description 2
239000010865 sewage Substances 0.000 description 2
235000015170 shellfish Nutrition 0.000 description 2
239000012085 test solution Substances 0.000 description 2
DGQOCLATAPFASR-UHFFFAOYSA-N tetrahydroxy-1,4-benzoquinone Chemical compound OC1=C(O)C(=O)C(O)=C(O)C1=O DGQOCLATAPFASR-UHFFFAOYSA-N 0.000 description 2
239000013598 vector Substances 0.000 description 2
239000003643 water by type Substances 0.000 description 2
FDOKWKTVAJNFLT-UHFFFAOYSA-N 2,5-dihydroxy-3,6-dinitrocyclohexa-2,5-diene-1,4-dione Chemical compound OC1=C([N+]([O-])=O)C(=O)C(O)=C([N+]([O-])=O)C1=O FDOKWKTVAJNFLT-UHFFFAOYSA-N 0.000 description 1
JKNCOURZONDCGV-UHFFFAOYSA-N 2-(dimethylamino)ethyl 2-methylprop-2-enoate Chemical compound CN(C)CCOC(=O)C(C)=C JKNCOURZONDCGV-UHFFFAOYSA-N 0.000 description 1
FPKCTSIVDAWGFA-UHFFFAOYSA-N 2-chloroanthracene-9,10-dione Chemical compound C1=CC=C2C(=O)C3=CC(Cl)=CC=C3C(=O)C2=C1 FPKCTSIVDAWGFA-UHFFFAOYSA-N 0.000 description 1
AERNLARMKHMKBX-UHFFFAOYSA-N 2-undecylcyclohexa-1,4-diene-1,4-diol Chemical compound CCCCCCCCCCCC1=C(O)CC=C(O)C1 AERNLARMKHMKBX-UHFFFAOYSA-N 0.000 description 1
MRVNKBNZHOHVER-UHFFFAOYSA-N 2h-anthracen-1-one Chemical compound C1=CC=C2C=C3C(=O)CC=CC3=CC2=C1 MRVNKBNZHOHVER-UHFFFAOYSA-N 0.000 description 1
BGVCGTNXEKDVCB-UHFFFAOYSA-N 4-hydroxy-3-methylnaphthalene-1,2-dione Chemical compound C1=CC=C2C(=O)C(=O)C(C)=C(O)C2=C1 BGVCGTNXEKDVCB-UHFFFAOYSA-N 0.000 description 1
WIRGBZBGYNIZIB-UHFFFAOYSA-N 4-hydroxy-6-methylchromen-2-one Chemical compound O1C(=O)C=C(O)C2=CC(C)=CC=C21 WIRGBZBGYNIZIB-UHFFFAOYSA-N 0.000 description 1
ODPOAESBSUKMHD-UHFFFAOYSA-L 6,7-dihydrodipyrido[1,2-b:1',2'-e]pyrazine-5,8-diium;dibromide Chemical compound [Br-].[Br-].C1=CC=[N+]2CC[N+]3=CC=CC=C3C2=C1 ODPOAESBSUKMHD-UHFFFAOYSA-L 0.000 description 1
RZVHIXYEVGDQDX-UHFFFAOYSA-N 9,10-anthraquinone Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3C(=O)C2=C1 RZVHIXYEVGDQDX-UHFFFAOYSA-N 0.000 description 1
229940076442 9,10-anthraquinone Drugs 0.000 description 1
241000238876 Acari Species 0.000 description 1
241000242759 Actiniaria Species 0.000 description 1
241000238426 Anostraca Species 0.000 description 1
241000242757 Anthozoa Species 0.000 description 1
241001672739 Artemia salina Species 0.000 description 1
241000206761 Bacillariophyta Species 0.000 description 1
241001474374 Blennius Species 0.000 description 1
241000700670 Bryozoa Species 0.000 description 1
241000235847 Bythotrephes cederstroemi Species 0.000 description 1
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
235000014653 Carica parviflora Nutrition 0.000 description 1
241000242722 Cestoda Species 0.000 description 1
241000700686 Chaetognatha Species 0.000 description 1
241000195649 Chlorella <Chlorellales> Species 0.000 description 1
241000195651 Chlorella sp. Species 0.000 description 1
206010008631 Cholera Diseases 0.000 description 1
241000206751 Chrysophyceae Species 0.000 description 1
241000238571 Cladocera Species 0.000 description 1
241000237501 Crassostrea Species 0.000 description 1
241000700108 Ctenophora <comb jellyfish phylum> Species 0.000 description 1
241000193907 Dreissena Species 0.000 description 1
238000001061 Dunnett's test Methods 0.000 description 1
JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
241000239366 Euphausiacea Species 0.000 description 1
CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 1
241000233866 Fungi Species 0.000 description 1
241000224466 Giardia Species 0.000 description 1
240000007058 Halophila ovalis Species 0.000 description 1
WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 1
241000243320 Hydrozoa Species 0.000 description 1
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
241001149911 Isopoda Species 0.000 description 1
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
240000008790 Musa x paradisiaca Species 0.000 description 1
235000018290 Musa x paradisiaca Nutrition 0.000 description 1
241000237524 Mytilus Species 0.000 description 1
241000244206 Nematoda Species 0.000 description 1
241000341511 Nematodes Species 0.000 description 1
241000216208 Neogobius melanostomus Species 0.000 description 1
241000238590 Ostracoda Species 0.000 description 1
241000237503 Pectinidae Species 0.000 description 1
241001232546 Pfiesteria Species 0.000 description 1
241000594009 Phoxinus phoxinus Species 0.000 description 1
LULCPJWUGUVEFU-UHFFFAOYSA-N Phthiocol Natural products C1=CC=C2C(=O)C(C)=C(O)C(=O)C2=C1 LULCPJWUGUVEFU-UHFFFAOYSA-N 0.000 description 1
239000004743 Polypropylene Substances 0.000 description 1
241000216244 Proterorhinus marmoratus Species 0.000 description 1
241000785681 Sander vitreus Species 0.000 description 1
241000242583 Scyphozoa Species 0.000 description 1
241000287219 Serinus canaria Species 0.000 description 1
DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical class [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 1
241001415519 Thaliacea Species 0.000 description 1
241000242541 Trematoda Species 0.000 description 1
241000251555 Tunicata Species 0.000 description 1
241000397921 Turbellaria Species 0.000 description 1
241000251539 Vertebrata <Metazoa> Species 0.000 description 1
241000607598 Vibrio Species 0.000 description 1
241000700605 Viruses Species 0.000 description 1
229930003448 Vitamin K Natural products 0.000 description 1
NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
239000000654 additive Substances 0.000 description 1
230000002411 adverse Effects 0.000 description 1
239000003905 agrochemical Substances 0.000 description 1
208000007502 anemia Diseases 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
230000009286 beneficial effect Effects 0.000 description 1
235000013361 beverage Nutrition 0.000 description 1
230000003115 biocidal effect Effects 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
238000004061 bleaching Methods 0.000 description 1
235000012206 bottled water Nutrition 0.000 description 1
CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
229910052791 calcium Inorganic materials 0.000 description 1
239000011575 calcium Substances 0.000 description 1
229910000019 calcium carbonate Inorganic materials 0.000 description 1
235000010216 calcium carbonate Nutrition 0.000 description 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
230000015556 catabolic process Effects 0.000 description 1
230000009087 cell motility Effects 0.000 description 1
241000902900 cellular organisms Species 0.000 description 1
125000001309 chloro group Chemical group Cl* 0.000 description 1
229930002868 chlorophyll a Natural products 0.000 description 1
229930002869 chlorophyll b Natural products 0.000 description 1
NSMUHPMZFPKNMZ-VBYMZDBQSA-M chlorophyll b Chemical compound C1([C@@H](C(=O)OC)C(=O)C2=C3C)=C2N2C3=CC(C(CC)=C3C=O)=[N+]4C3=CC3=C(C=C)C(C)=C5N3[Mg-2]42[N+]2=C1[C@@H](CCC(=O)OC\C=C(/C)CCC[C@H](C)CCC[C@H](C)CCCC(C)C)[C@H](C)C2=C5 NSMUHPMZFPKNMZ-VBYMZDBQSA-M 0.000 description 1
210000003763 chloroplast Anatomy 0.000 description 1
230000001684 chronic effect Effects 0.000 description 1
238000010960 commercial process Methods 0.000 description 1
238000011109 contamination Methods 0.000 description 1
229960000956 coumarin Drugs 0.000 description 1
230000006378 damage Effects 0.000 description 1
238000006731 degradation reaction Methods 0.000 description 1
230000001627 detrimental effect Effects 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
201000010099 disease Diseases 0.000 description 1
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
239000003651 drinking water Substances 0.000 description 1
235000013399 edible fruits Nutrition 0.000 description 1
238000000295 emission spectrum Methods 0.000 description 1
230000007613 environmental effect Effects 0.000 description 1
238000001317 epifluorescence microscopy Methods 0.000 description 1
SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
238000000605 extraction Methods 0.000 description 1
238000010566 fecundity assay Methods 0.000 description 1
238000001914 filtration Methods 0.000 description 1
239000000796 flavoring agent Substances 0.000 description 1
235000019634 flavors Nutrition 0.000 description 1
230000002496 gastric effect Effects 0.000 description 1
210000002149 gonad Anatomy 0.000 description 1
230000012447 hatching Effects 0.000 description 1
230000007062 hydrolysis Effects 0.000 description 1
238000006460 hydrolysis reaction Methods 0.000 description 1
238000005286 illumination Methods 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
230000005764 inhibitory process Effects 0.000 description 1
238000011081 inoculation Methods 0.000 description 1
YWXYYJSYQOXTPL-SLPGGIOYSA-N isosorbide mononitrate Chemical compound [O-][N+](=O)O[C@@H]1CO[C@@H]2[C@@H](O)CO[C@@H]21 YWXYYJSYQOXTPL-SLPGGIOYSA-N 0.000 description 1
230000002045 lasting effect Effects 0.000 description 1
239000007788 liquid Substances 0.000 description 1
229910052749 magnesium Inorganic materials 0.000 description 1
239000011777 magnesium Substances 0.000 description 1
235000013372 meat Nutrition 0.000 description 1
125000005395 methacrylic acid group Chemical group 0.000 description 1
238000000386 microscopy Methods 0.000 description 1
239000003595 mist Substances 0.000 description 1
238000012986 modification Methods 0.000 description 1
230000004048 modification Effects 0.000 description 1
239000000178 monomer Substances 0.000 description 1
230000021616 negative regulation of cell division Effects 0.000 description 1
235000015097 nutrients Nutrition 0.000 description 1
230000000050 nutritive effect Effects 0.000 description 1
230000003647 oxidation Effects 0.000 description 1
238000007254 oxidation reaction Methods 0.000 description 1
230000004792 oxidative damage Effects 0.000 description 1
238000006385 ozonation reaction Methods 0.000 description 1
125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
229960000280 phenindione Drugs 0.000 description 1
230000000243 photosynthetic effect Effects 0.000 description 1
XKJCHHZQLQNZHY-UHFFFAOYSA-N phthalimide Chemical compound C1=CC=C2C(=O)NC(=O)C2=C1 XKJCHHZQLQNZHY-UHFFFAOYSA-N 0.000 description 1
SHUZOJHMOBOZST-UHFFFAOYSA-N phylloquinone Natural products CC(C)CCCCC(C)CCC(C)CCCC(=CCC1=C(C)C(=O)c2ccccc2C1=O)C SHUZOJHMOBOZST-UHFFFAOYSA-N 0.000 description 1
239000000049 pigment Substances 0.000 description 1
229920000768 polyamine Polymers 0.000 description 1
239000004417 polycarbonate Substances 0.000 description 1
229920000515 polycarbonate Polymers 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
229920001155 polypropylene Polymers 0.000 description 1
239000000047 product Substances 0.000 description 1
230000002062 proliferating effect Effects 0.000 description 1
108090000623 proteins and genes Proteins 0.000 description 1
102000004169 proteins and genes Human genes 0.000 description 1
238000000746 purification Methods 0.000 description 1
239000010453 quartz Substances 0.000 description 1
230000009467 reduction Effects 0.000 description 1
230000002829 reductive effect Effects 0.000 description 1
230000004044 response Effects 0.000 description 1
238000012428 routine sampling Methods 0.000 description 1
239000000523 sample Substances 0.000 description 1
235000020637 scallop Nutrition 0.000 description 1
239000013535 sea water Substances 0.000 description 1
VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
239000002002 slurry Substances 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000000243 solution Substances 0.000 description 1
230000000087 stabilizing effect Effects 0.000 description 1
238000004659 sterilization and disinfection Methods 0.000 description 1
239000000758 substrate Substances 0.000 description 1
239000006228 supernatant Substances 0.000 description 1
230000004083 survival effect Effects 0.000 description 1
230000002459 sustained effect Effects 0.000 description 1
230000009182 swimming Effects 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
241001223854 teleost fish Species 0.000 description 1
238000009210 therapy by ultrasound Methods 0.000 description 1
238000007669 thermal treatment Methods 0.000 description 1
239000003053 toxin Substances 0.000 description 1
231100000765 toxin Toxicity 0.000 description 1
108700012359 toxins Proteins 0.000 description 1
238000009281 ultraviolet germicidal irradiation Methods 0.000 description 1
235000013311 vegetables Nutrition 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
229920002554 vinyl polymer Polymers 0.000 description 1
235000019168 vitamin K Nutrition 0.000 description 1
239000011712 vitamin K Substances 0.000 description 1
150000003721 vitamin K derivatives Chemical class 0.000 description 1
229940046010 vitamin k Drugs 0.000 description 1
239000002351 wastewater Substances 0.000 description 1

Classifications

- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N35/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical
- A01N35/06—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical containing keto or thioketo groups as part of a ring, e.g. cyclohexanone, quinone; Derivatives thereof, e.g. ketals
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof
- A01N37/32—Cyclic imides of polybasic carboxylic acids or thio analogues thereof
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
- A01N43/14—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom six-membered rings
- A01N43/16—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom six-membered rings with oxygen as the ring hetero atom
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/50—Treatment of water, waste water, or sewage by addition or application of a germicide or by oligodynamic treatment
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2103/00—Nature of the water, waste water, sewage or sludge to be treated
- C02F2103/008—Originating from marine vessels, ships and boats, e.g. bilge water or ballast water
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2303/00—Specific treatment goals
- C02F2303/04—Disinfection

Landscapes

Life Sciences & Earth Sciences (AREA)
Engineering & Computer Science (AREA)
Health & Medical Sciences (AREA)
Environmental Sciences (AREA)
Zoology (AREA)
Wood Science & Technology (AREA)
General Health & Medical Sciences (AREA)
Dentistry (AREA)
Agronomy & Crop Science (AREA)
Plant Pathology (AREA)
Pest Control & Pesticides (AREA)
Organic Chemistry (AREA)
Chemical & Material Sciences (AREA)
Water Supply & Treatment (AREA)
Environmental & Geological Engineering (AREA)
Hydrology & Water Resources (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Farming Of Fish And Shellfish (AREA)
Catching Or Destruction (AREA)

CA2406968A 2000-02-17 2001-02-16 Method of controlling zoological and aquatic plant growth Expired - Fee Related CA2406968C (en)

Applications Claiming Priority (5)

Application Number	Priority Date	Filing Date	Title
US09/506,017		2000-02-17
US09/506,017 US6340468B1 (en)	2000-02-17	2000-02-17	Method of controlling zoological and aquatic plant growth
US23740100P	2000-10-04	2000-10-04
US60/237,401		2000-10-04
PCT/US2001/005117 WO2001060971A2 (en)	2000-02-17	2001-02-16	Method of controlling zoological and aquatic plant growth

Publications (2)

Publication Number	Publication Date
CA2406968A1 CA2406968A1 (en)	2001-08-23
CA2406968C true CA2406968C (en)	2011-07-05

Family

ID=26930638

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA2406968A Expired - Fee Related CA2406968C (en)	2000-02-17	2001-02-16	Method of controlling zoological and aquatic plant growth

Country Status (29)

Country	Link
US (2)	US6576674B2 (de)
EP (3)	EP2130436A1 (de)
JP (1)	JP2003523821A (de)
KR (3)	KR100898815B1 (de)
CN (1)	CN1424875B (de)
AP (1)	AP1487A (de)
AT (1)	ATE441327T1 (de)
AU (2)	AU2001241530B2 (de)
BG (1)	BG107108A (de)
CA (1)	CA2406968C (de)
CU (1)	CU23320A3 (de)
DE (1)	DE60139763D1 (de)
DK (1)	DK1261254T3 (de)
DZ (1)	DZ3294A1 (de)
EA (1)	EA006842B1 (de)
EE (1)	EE04984B1 (de)
ES (1)	ES2331645T3 (de)
GE (1)	GEP20053561B (de)
HR (1)	HRP20020754A2 (de)
IL (1)	IL151306A (de)
IS (1)	IS6506A (de)
MA (1)	MA26045A1 (de)
MX (1)	MXPA02008019A (de)
NO (1)	NO331276B1 (de)
NZ (1)	NZ531864A (de)
OA (1)	OA12217A (de)
PL (1)	PL207835B1 (de)
WO (1)	WO2001060971A2 (de)
YU (1)	YU61902A (de)

Families Citing this family (28)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US6626122B2 (en)	2001-10-18	2003-09-30	Chevron U.S.A. Inc	Deactivatable biocides in ballast water
US6800615B2 (en)	2002-04-15	2004-10-05	Board Of Trustees Of Michigan State University	Antihelminthic anthraquinones and method of use thereof
US6949250B2 (en) *	2002-12-16	2005-09-27	The United States Of America As Represented By The Secretary Of Agriculture	Selective algaecides for control of cyanochloronta
JP4619614B2 (ja) *	2002-12-16	2011-01-26	中部電力株式会社	藍藻類・地衣類の繁藻抑制剤
BR0317589B1 (pt) *	2002-12-20	2014-10-14	Lonza Ag	"método para desintegração da película biológica aderida a substrato em meio aquoso".
JP4167096B2 (ja) *	2003-03-13	2008-10-15	関西電力株式会社	ポリプの除去又は増殖抑制方法
ITMI20031011A1 (it) *	2003-05-20	2004-11-21	Vanetta S P A	Composti biocidi per il trattamento delle acque.
JP2005139125A (ja) *	2003-11-07	2005-06-02	Agro Kanesho Co Ltd	ジャンボタニシ駆除剤
WO2005067986A1 (en) *	2004-01-07	2005-07-28	Noxilizer, Inc.	Sterilization system and device
US8017074B2 (en) *	2004-01-07	2011-09-13	Noxilizer, Inc.	Sterilization system and device
US7258878B2 (en)	2004-12-20	2007-08-21	Kimberly-Clark Worldwide, Inc.	Anti-microbial composition and methods of use thereof
US20080014145A1 (en) *	2006-07-11	2008-01-17	David Joseph Anschel	Abalone settlement bioassay for anti-seizure substance screening
CN101536687B (zh) *	2008-03-20	2013-12-18	香港科技大学	黄酮和异黄酮衍生物作为抗生物污损物质的应用以及防止海洋生物污损的方法和涂料
KR101013946B1 (ko) *	2008-05-02	2011-02-14	한국화학연구원	메나디온계 화합물을 포함하는 유해조류 방제용 조성물 및이를 이용한 유해조류 방제방법
KR101024606B1 (ko) *	2008-05-20	2011-03-24	한국화학연구원	천연물 유래의 안트라퀴논계 화합물을 함유하는 유해조류방제용 혼합조성물과 이를 이용한 방제방법
WO2010071804A1 (en) *	2008-12-18	2010-06-24	Keith Branly	Formulations of broad spectrum biocides and their use in improved methods for the treatment of ballast water
GB0901434D0 (en)	2009-01-29	2009-03-11	Univ Strathclyde	Ballast water treatment system
BRPI1008696A2 (pt) *	2009-02-17	2016-03-08	Mcalister Technologies Llc	célula eletrolítica e método para usar a mesma.
EP2517736B1 (de)	2009-02-23	2014-03-26	Noxilizer, Inc.	Vorrichtung zur Gassterilisation
KR101436792B1 (ko) *	2011-07-08	2014-09-05	한양대학교 산학협력단	나프토퀴논 화합물을 함유하는 유해조류 제어용 조성물
ES2569719T3 (es) *	2011-08-17	2016-05-12	Buckman Laboratories International, Inc	Métodos para controlar el crecimiento de costra o incrustación en sistemas acuosos
KR101405275B1 (ko)	2012-02-28	2014-06-11	조선대학교산학협력단	나프토퀴논 유도체를 유효성분으로 포함하는 적조 방제용 조성물
CN103651349A (zh) *	2013-09-07	2014-03-26	宁波市雨辰环保科技有限公司	蒽醌盐在制备用于杀菌或去除甲醛的消毒剂中的应用
RU2563283C2 (ru) *	2013-12-03	2015-09-20	Федеральное государственное бюджетное научное учреждение "Азовский научно-исследовательский институт рыбного хозяйства" (ФГБНУ "АзНИИРХ")	Способ оценки токсичности загрязнителей вод азово-черноморского бассейна
KR101829962B1 (ko) *	2015-12-03	2018-02-19	한양대학교 산학협력단	나프토퀴논 유도체를 포함하는 유해조류 제어용 조성물 및 이를 이용한 유해조류 제어방법
ES2603380B1 (es)	2017-01-17	2017-09-12	Ox-Cta, S.L.	Equipo y procedimiento de detección de protozoos
WO2018152416A1 (en) *	2017-02-16	2018-08-23	Jon Baker	Systems and methods for controlling aquatic pests with sulfurous acid
CN108676066B (zh) *	2018-05-29	2021-09-10	深圳大学	一种化合物Malformin C的应用及制备方法

Family Cites Families (35)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2999810A (en)	1959-06-24	1961-09-12	Us Rubber Co	Method of killing algae
US3558787A (en) *	1968-01-23	1971-01-26	Du Pont	Methods and compositions for controlling plant-pathogenic fungi utilizing 1,4-dihydro-9,10-anthraquinones
US3947594A (en) *	1973-05-07	1976-03-30	Gaf Corporation	4-Halo-1-hydroxyanthraquinone containing fungicidal composition
US4092433A (en) *	1976-03-08	1978-05-30	Abbott Laboratories	Quinone derivatives as molluscicides
US4238484A (en) *	1979-04-27	1980-12-09	Abbott Laboratories	Molluscicide compositions and methods of use
JPS5738704A (en) *	1980-08-21	1982-03-03	Asahi Chem Ind Co Ltd	Antifouling agent
JPS5931396B2 (ja) *	1981-06-12	1984-08-01	東海電化工業株式会社	溶存酸素除去法
JPS58120678A (ja)	1982-01-12	1983-07-18	Mitsubishi Rayon Co Ltd	防汚塗料用組成物
FR2588442B1 (fr) *	1985-10-11	1989-02-17	Rhone Poulenc Agrochimie	Semences de riz enrobees d'algicide et procede de culture du riz
JPS6431702A (en)	1987-07-28	1989-02-02	Ihara Chemical Ind Co	Repellent for aquatic attached organism
JPH024701A (ja) *	1988-06-24	1990-01-09	Ihara Chem Ind Co Ltd	キノン誘導体を有効成分とする水中生物防汚剤
CA2020826A1 (en)	1989-07-11	1991-01-12	Junji Yokoi	Antifouling composition
DE4013023A1 (de) *	1990-04-24	1991-11-07	Lohmann Rudolf Lomapharm	Verwendung von anthrachinonderivaten zur prophylaxe und therapie von viruserkrankungen
US5252330A (en)	1990-10-12	1993-10-12	University Of Toledo	Method of controling zebra mussels with extract of Phytolacca dodecandra
JPH04322788A (ja) *	1991-02-25	1992-11-12	Mitsubishi Heavy Ind Ltd	船舶のバラスト水殺菌方法および殺菌装置
US5128050A (en)	1991-05-06	1992-07-07	Calgon Corporation	Method for controlling zebra mussels in ship ballast tanks
US5192451A (en)	1991-05-06	1993-03-09	Calgon Corporation	Method for controlling zebra mussels in ship ballast tanks
US5160047A (en)	1992-02-18	1992-11-03	Nalco Chemical Company	Glutaraldehyde for controlling Zebra mussels
US6080791A (en) *	1992-07-24	2000-06-27	Seres Laboratories, Inc.	Method of treating a viral condition by inhibiting membrane fusion
CN1054116C (zh) *	1992-10-02	2000-07-05	生物技术资源两合公司	用作硫酸盐还原菌产生硫化物的抑制剂的细分散蒽醌类制剂
US5288693A (en) *	1993-06-25	1994-02-22	Rohm And Haas Company	2-(3-oxoalk(en)yl)-3-isothiazolones and derivatives as antimicrobial agents
US5851408A (en)	1997-01-24	1998-12-22	Sedivy; John Joseph	Elimination and inhibition of bivalve mollusk attachments
KR19980067751A (ko) *	1996-02-12	1998-10-15	맥더못 엘리라 베즈엘	쌍각류 연체동물 부착물의 제거 및 방지
AUPN859096A0 (en) *	1996-03-11	1996-04-04	Archer, Walter James	Ballast water de-toxification treatment system for ships
US5932112A (en) *	1996-11-27	1999-08-03	Browning Transport Management, Inc.	Method and apparatus for killing microorganisms in ship ballast water
DE69801499T2 (de) *	1997-05-12	2002-04-18	Dcv, Inc.	Verfahren zur verminderung des schwefelwasserstoffgehaltes in einem abwassersystem
JPH1133583A (ja) *	1997-07-17	1999-02-09	Nippon Soda Co Ltd	活性汚泥のバルキング防除剤及び防除方法
US5900157A (en)	1997-07-18	1999-05-04	Betzdearborn Inc.	Methods for controlling macroinvertebrates in aqueous systems
BR9815550A (pt) *	1997-07-29	2000-10-31	Dcv Inc	Método não biocida para inibir a geração de sulfeto biogênico
JPH11156383A (ja) *	1997-11-21	1999-06-15	Ryoji Saeki	水浄化用組成物、水浄化法およびそれらを利用した水浄化システム
US5976229A (en)	1998-01-28	1999-11-02	Kyosei Chemicals Co., Ltd.	Underwater anti-fouling agent and anti-fouling paint containing the underwater anti-fouling agent
US6164244A (en)	1998-03-20	2000-12-26	Pharmacognetics, Inc.	Method for treating aquatic pests
JP2000034202A (ja) *	1998-07-15	2000-02-02	Kawasaki Kasei Chem Ltd	硫酸塩還元菌による硫化物生成の抑制方法
US6340468B1 (en)	2000-02-17	2002-01-22	Garnett, Inc.	Method of controlling zoological and aquatic plant growth
SV2003000753A (es) *	2000-12-05	2003-06-16	Brigham & Womens Hospital	Uso de polisacaridos zwitterionicos para la especifica modulacion del progreso inmunologico

2001
- 2001-02-16 DK DK01912784T patent/DK1261254T3/da active
- 2001-02-16 JP JP2001560343A patent/JP2003523821A/ja active Pending
- 2001-02-16 IL IL151306A patent/IL151306A/en not_active IP Right Cessation
- 2001-02-16 HR HR20020754A patent/HRP20020754A2/hr not_active Application Discontinuation
- 2001-02-16 WO PCT/US2001/005117 patent/WO2001060971A2/en not_active Ceased
- 2001-02-16 YU YU61902A patent/YU61902A/sh unknown
- 2001-02-16 CA CA2406968A patent/CA2406968C/en not_active Expired - Fee Related
- 2001-02-16 DZ DZ013294A patent/DZ3294A1/de active
- 2001-02-16 PL PL361808A patent/PL207835B1/pl not_active IP Right Cessation
- 2001-02-16 NZ NZ531864A patent/NZ531864A/en not_active IP Right Cessation
- 2001-02-16 AU AU2001241530A patent/AU2001241530B2/en not_active Ceased
- 2001-02-16 AP APAP/P/2002/002625A patent/AP1487A/en active
- 2001-02-16 OA OA1200200253A patent/OA12217A/en unknown
- 2001-02-16 EA EA200200867A patent/EA006842B1/ru not_active IP Right Cessation
- 2001-02-16 GE GE4894A patent/GEP20053561B/en unknown
- 2001-02-16 EP EP09165593A patent/EP2130436A1/de not_active Withdrawn
- 2001-02-16 MX MXPA02008019A patent/MXPA02008019A/es active IP Right Grant
- 2001-02-16 DE DE60139763T patent/DE60139763D1/de not_active Expired - Lifetime
- 2001-02-16 KR KR1020087001280A patent/KR100898815B1/ko not_active Expired - Fee Related
- 2001-02-16 KR KR1020087001279A patent/KR100964351B1/ko not_active Expired - Fee Related
- 2001-02-16 ES ES01912784T patent/ES2331645T3/es not_active Expired - Lifetime
- 2001-02-16 EP EP09165594A patent/EP2105050A1/de not_active Withdrawn
- 2001-02-16 CN CN018082491A patent/CN1424875B/zh not_active Expired - Fee Related
- 2001-02-16 KR KR1020027010718A patent/KR100865788B1/ko not_active Expired - Fee Related
- 2001-02-16 AU AU4153001A patent/AU4153001A/xx active Pending
- 2001-02-16 AT AT01912784T patent/ATE441327T1/de not_active IP Right Cessation
- 2001-02-16 EE EEP200200455A patent/EE04984B1/xx not_active IP Right Cessation
- 2001-02-16 EP EP01912784A patent/EP1261254B1/de not_active Expired - Lifetime
- 2001-12-06 US US10/003,464 patent/US6576674B2/en not_active Expired - Fee Related
- 2001-12-06 US US10/003,465 patent/US7348363B2/en not_active Expired - Fee Related
2002
- 2002-08-15 IS IS6506A patent/IS6506A/is unknown
- 2002-08-16 NO NO20023912A patent/NO331276B1/no not_active IP Right Cessation
- 2002-08-16 CU CU20020174A patent/CU23320A3/es not_active IP Right Cessation
- 2002-09-16 MA MA26823A patent/MA26045A1/fr unknown
- 2002-09-16 BG BG107108A patent/BG107108A/bg unknown

Also Published As

Publication number	Publication date
KR100865788B1 (ko)	2008-10-29
YU61902A (sh)	2006-01-16
EA006842B1 (ru)	2006-04-28
KR20080009341A (ko)	2008-01-28
ATE441327T1 (de)	2009-09-15
WO2001060971A3 (en)	2001-12-13
US20020098978A1 (en)	2002-07-25
NZ531864A (en)	2006-02-24
EP1261254A2 (de)	2002-12-04
EP2105050A1 (de)	2009-09-30
KR100898815B1 (ko)	2009-05-22
CN1424875B (zh)	2012-10-03
EP1261254B1 (de)	2009-09-02
EP1261254A4 (de)	2005-11-23
KR20020087400A (ko)	2002-11-22
EE04984B1 (et)	2008-04-15
NO331276B1 (no)	2011-11-14
DZ3294A1 (de)	2001-08-23
EP2130436A1 (de)	2009-12-09
AU2001241530B2 (en)	2006-03-02
ES2331645T3 (es)	2010-01-12
JP2003523821A (ja)	2003-08-12
IL151306A0 (en)	2003-04-10
EE200200455A (et)	2003-12-15
PL361808A1 (en)	2004-10-04
US7348363B2 (en)	2008-03-25
KR20080011246A (ko)	2008-01-31
HRP20020754A2 (en)	2005-02-28
GEP20053561B (en)	2005-07-11
CA2406968A1 (en)	2001-08-23
HK1052836A1 (en)	2003-10-03
IS6506A (is)	2002-08-15
NO20023912L (no)	2002-10-07
CU23320A3 (es)	2008-10-22
AU4153001A (en)	2001-08-27
DE60139763D1 (de)	2009-10-15
PL207835B1 (pl)	2011-02-28
WO2001060971A2 (en)	2001-08-23
AP1487A (en)	2005-11-29
CN1424875A (zh)	2003-06-18
MA26045A1 (fr)	2004-04-01
MXPA02008019A (es)	2004-09-06
US20020098979A1 (en)	2002-07-25
AP2002002625A0 (en)	2002-09-30
OA12217A (en)	2006-05-09
US6576674B2 (en)	2003-06-10
EA200200867A1 (ru)	2003-06-26
NO20023912D0 (no)	2002-08-16
BG107108A (bg)	2003-04-30
IL151306A (en)	2007-03-08
DK1261254T3 (da)	2010-01-04
KR100964351B1 (ko)	2010-06-17

Legal Events

Date	Code	Title	Description
2006-02-13	EEER	Examination request
2014-04-01	MKLA	Lapsed	Effective date: 20140218

Publication	Publication Date	Title
CA2406968C (en)	2011-07-05	Method of controlling zoological and aquatic plant growth
AU2001241530A1 (en)	2001-11-08	Method of controlling zoological and aquatic plant growth
US6284793B1 (en)	2001-09-04	Process for preventing contamination of the aquatic environment with organisms from ballast water
US6340468B1 (en)	2002-01-22	Method of controlling zoological and aquatic plant growth
US20030012804A1 (en)	2003-01-16	Aquacide and use
US6164244A (en)	2000-12-26	Method for treating aquatic pests
US20100000457A1 (en)	2010-01-07	Method of controlling zoological and aquatic plant growth
Matsuyama et al.	1999	Effects of harmful dinoflagellates, Gymnodinium mikimotoi and Heterocapsa circularisquama, red-tide on filtering rate of bivalve molluscs
US20040232089A1 (en)	2004-11-25	Biocidal compounds for treating water
Faimali et al.	2006	A new photodegradable molecule as a low impact ballast water biocide: efficacy screening on marine organisms from different trophic levels
HK1133791A (en)	2010-04-09	Method of controlling zoological and aquatic plant growth
HK1133790A (en)	2010-04-09	Method of controlling zoological and aquatic plant growth
HK1052836B (en)	2010-04-09	Method of controlling zoological and aquatic plant growth
GAVAND et al.	0	AN EVALUATION OF SONICATION AND ADVANCED CHEMICAL OXIDANT TREATMENTS AS A MECHANISM TO ERADICATE BALLAST-BORNE UNICELLULAR ALGAE USING DUNALIELLA TERTIOLECTA AS A MODEL ALGA